Functional analysis of mutations in the human carnitine/acylcarnitine translocase in Aspergillus nidulans

This publication has 32 references indexed in Scilit:

• Aberrant mRNA Splicing Associated with Coding Region Mutations in Children with Carnitine-Acylcarnitine Translocase Deficiency
  Molecular Genetics and Metabolism, 2001
• The Aspergillus nidulans carnitine carrier encoded by the acuH gene is exclusively located in the mitochondria
  FEMS Microbiology Letters, 2001
• The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism
  American Journal of Human Genetics, 2001
• The acuH gene of Aspergillus nidulans , required for growth on acetate and long-chain fatty acids, encodes a putative homologue of the mammalian carnitine/acylcarnitine carrier
  Archiv für Mikrobiologie, 1999
• Murine modelling of classical lissencephaly
  neurogenetics, 1999
• Characterization of oleate-nonutilizing mutants of Aspergillus nidulans isolated by the 3-amino-1,2,4-triazole positive selection method
  Archiv für Mikrobiologie, 1997
• The molecular basis of alkaptonuria
  Nature Genetics, 1996
• Fungal metabolic model for human type I hereditary tyrosinaemia.
  Proceedings of the National Academy of Sciences, 1995
• Analysis of the regulation of the Aspergillus nidulans acuD gene, encoding isocitrate lyase, by construction of a hybrid promoter
  Molecular Genetics and Genomics, 1994
• Analysis of Acetate Non-utilizing (acu) Mutants in Aspergillus nidulans
  Journal of General Microbiology, 1976